The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
127691921 12769192 1 I 20160607 20160914 20160921 20160921 EXP GB-AMGEN-GBRCT2016125433 AMGEN 0.00 F Y 0.00000 20160921 OT GB GB

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
127691921 12769192 1 PS carfilzomib CARFILZOMIB 1 Intravenous (not otherwise specified) 70 MG, PER CHEMO REGIM 202714 70 MG INTRAVENOUS INFUSION
127691921 12769192 2 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Oral 500 MG, PER CHEMO REGIM 0 500 MG UNKNOWN FORMULATION
127691921 12769192 3 SS DEXAMETHASONE. DEXAMETHASONE 1 Oral 20 MG, PER CHEMO REGIM 0 20 MG UNKNOWN FORMULATION
127691921 12769192 4 SS DAPSONE. DAPSONE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127691921 12769192 1 Plasma cell myeloma
127691921 12769192 2 Plasma cell myeloma
127691921 12769192 3 Plasma cell myeloma
127691921 12769192 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127691921 12769192 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127691921 12769192 Methaemoglobinaemia

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127691921 12769192 1 20160511 0
127691921 12769192 2 20160511 0
127691921 12769192 3 20160511 0